Innovative
and responsible Pharmaceuticals

16+

years of experiance in pharmacy

60+

export countries

10+

developed technologies

100+

workforce

1 million

annual sterile vials produced

Who are we

PharmIdea is a company certified in Good Manufacturing Practice by the European Union and internationally recognized for the production of sterile drugs, located in Latvia. We have more than 15 years of experience in the development of sterile drug technologies, preparation of documentation, and drug manufacturing. Our services include the development, production, registration of finished pharmaceuticals, and product sales in more than 60 international markets.

We specialize in the development and production of sterile drugs. The PharmIdea product range includes generic medications in therapeutic groups such as oncology, obstetrics, antifungal, cardiology, and anesthesia drugs. We pride ourselves on being able to find solutions for our clients’ individual needs by developing technology and preparing technical documentation in accordance with the requirements of authorities in many countries around the world, while maintaining the priority to ensure drug production according to European Union quality standards.

The company’s growth has been possible thanks to our team of more than 100 industry professionals. Together, we have created a friendly, open, and safe work environment that strives for improvement and excellence. PharmIdea constantly promotes individual growth and nurtures the talents of its employees to ensure the team comprises highly qualified, responsible, and in-demand professionals in the industry.

Sterile dosage forms

We develop and manufacture sterile drugs in vials, ensuring that our injectable products meet the highest quality standards across various therapeutic groups, including oncology, fungal infections, cardiology, anesthesia, and others.

Continuous development

We continuously monitor and adapt to the growing demands and current trends of the industry by improving technological processes, updating documentation, training staff, enhancing team competencies, and expanding our scope of operations.

From idea to sale

We provide a comprehensive full-service cycle for the development, production, preparation of registration documentation, and support during the process for sterile drug forms. We manufacture batches according to customer orders, performing complete analytical testing, quality control, and issuing certificates of compliance. We package, serialize, and deliver the finished pharmaceutical product to the customer in accordance with the registered documentation.

Development

We offer our clients the opportunity to complete the full product cycle, starting with the qualification of the active substance, development of technology, production of validation batches, stability studies, and preparation of documentation for drug registration in European and other markets.

MANUFACTURING

Pharmidea manufactures generic medications in sterile vials, utilizing various technological methods – lyophilization, aseptic filling, and autoclaving.

Licensing

We offer developed technical documentation for the registration of generic products that complies with EMA and ICH guidelines. During the drug registration process, we provide support and adjust the documentation in accordance with the requirements of the client’s country’s authorities.

INVESTIGATIONAL DRUG DEVELOPMENT AND MANUFACTURING

We have a license and experience in improving the formulation of investigational drugs, developing technology in the laboratory, and preparing documentation for Phase I-III clinical trials.

Take the next career step and join innovative pharmaceuticals

Join our team! We offer employment in a dynamic environment with ample opportunities to develop skills and advance qualifications for both seasoned industry professionals and emerging talents.